rs144673025
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs144673025(C;C) |
| Make rs144673025(C;T) |
| Make rs144673025(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 223004684 |
| Gene | DISP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs144673025 |
| dbSNP (classic) | rs144673025 |
| ClinGen | rs144673025 |
| ebi | rs144673025 |
| HLI | rs144673025 |
| Exac | rs144673025 |
| Gnomad | rs144673025 |
| Varsome | rs144673025 |
| LitVar | rs144673025 |
| Map | rs144673025 |
| PheGenI | rs144673025 |
| Biobank | rs144673025 |
| 1000 genomes | rs144673025 |
| hgdp | rs144673025 |
| ensembl | rs144673025 |
| geneview | rs144673025 |
| scholar | rs144673025 |
| rs144673025 | |
| pharmgkb | rs144673025 |
| gwascentral | rs144673025 |
| openSNP | rs144673025 |
| 23andMe | rs144673025 |
| SNPshot | rs144673025 |
| SNPdbe | rs144673025 |
| MSV3d | rs144673025 |
| GWAS Ctlg | rs144673025 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
